US20090060785A1 - Automatic multi-purpose analyzer - Google Patents
Automatic multi-purpose analyzer Download PDFInfo
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- US20090060785A1 US20090060785A1 US12/200,459 US20045908A US2009060785A1 US 20090060785 A1 US20090060785 A1 US 20090060785A1 US 20045908 A US20045908 A US 20045908A US 2009060785 A1 US2009060785 A1 US 2009060785A1
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- sample
- pipetting
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- analysis
- liquid surface
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N35/10—Devices for transferring samples or any liquids to, in, or from, the analysis apparatus, e.g. suction devices, injection devices
- G01N35/1009—Characterised by arrangements for controlling the aspiration or dispense of liquids
- G01N35/1011—Control of the position or alignment of the transfer device
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01F—MEASURING VOLUME, VOLUME FLOW, MASS FLOW OR LIQUID LEVEL; METERING BY VOLUME
- G01F23/00—Indicating or measuring liquid level or level of fluent solid material, e.g. indicating in terms of volume or indicating by means of an alarm
- G01F23/22—Indicating or measuring liquid level or level of fluent solid material, e.g. indicating in terms of volume or indicating by means of an alarm by measuring physical variables, other than linear dimensions, pressure or weight, dependent on the level to be measured, e.g. by difference of heat transfer of steam or water
- G01F23/26—Indicating or measuring liquid level or level of fluent solid material, e.g. indicating in terms of volume or indicating by means of an alarm by measuring physical variables, other than linear dimensions, pressure or weight, dependent on the level to be measured, e.g. by difference of heat transfer of steam or water by measuring variations of capacity or inductance of capacitors or inductors arising from the presence of liquid or fluent solid material in the electric or electromagnetic fields
- G01F23/263—Indicating or measuring liquid level or level of fluent solid material, e.g. indicating in terms of volume or indicating by means of an alarm by measuring physical variables, other than linear dimensions, pressure or weight, dependent on the level to be measured, e.g. by difference of heat transfer of steam or water by measuring variations of capacity or inductance of capacitors or inductors arising from the presence of liquid or fluent solid material in the electric or electromagnetic fields by measuring variations in capacitance of capacitors
- G01F23/265—Indicating or measuring liquid level or level of fluent solid material, e.g. indicating in terms of volume or indicating by means of an alarm by measuring physical variables, other than linear dimensions, pressure or weight, dependent on the level to be measured, e.g. by difference of heat transfer of steam or water by measuring variations of capacity or inductance of capacitors or inductors arising from the presence of liquid or fluent solid material in the electric or electromagnetic fields by measuring variations in capacitance of capacitors for discrete levels
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N35/10—Devices for transferring samples or any liquids to, in, or from, the analysis apparatus, e.g. suction devices, injection devices
- G01N35/1009—Characterised by arrangements for controlling the aspiration or dispense of liquids
- G01N2035/1025—Fluid level sensing
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/2041—Two or more non-extruded coatings or impregnations
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/2041—Two or more non-extruded coatings or impregnations
- Y10T442/2049—Each major face of the fabric has at least one coating or impregnation
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/2041—Two or more non-extruded coatings or impregnations
- Y10T442/2049—Each major face of the fabric has at least one coating or impregnation
- Y10T442/2057—At least two coatings or impregnations of different chemical composition
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
- Y10T442/2041—Two or more non-extruded coatings or impregnations
- Y10T442/2049—Each major face of the fabric has at least one coating or impregnation
- Y10T442/2057—At least two coatings or impregnations of different chemical composition
- Y10T442/2066—Different coatings or impregnations on opposite faces of the fabric
Definitions
- the present invention relates to an automatic multi-purpose analyzer which performs qualitative and quantitative analysis of biological samples such as blood, urine, etc. More particularly, the present invention relates to an automatic multi-purpose analyzer having a function for transferring a sample between a plurality of analysis units through a transfer apparatus.
- An object of the present invention is to provide an automatic modularized multi-purpose analyzer that attains higher throughput.
- the present invention is configured as follows:
- An automatic multi-purpose analyzer having a plurality of analysis units connected in series through a transfer line for transferring sample liquid, each of the analysis units including a pipetting mechanism for pipetting sample liquid, wherein each of the analysis units includes a transmission mechanism for transmitting information about the amount of a sample liquid to other analysis units, the information being obtained upon sample pipetting by the pipetting mechanism of each of the analysis units
- a mechanism used for first detecting the liquid surface to recognize its height (hereinafter referred to as surface height or surface level interchangeably) securely measures the surface height.
- Such a mechanism is based on a reliable liquid surface method.
- Information on the surface height is transferred to another analysis unit in which a capacitive sample probe is inserted into and then lowered inside a vessel. With the capacitive probe, capacitance fluctuation from a certain timing is monitored and, when the liquid surface is judged, lowering operation of the probe is stopped. This timing is referred to as reset time.
- reset time With a conventional analyzer, it is not possible to know the height of the vessel at which the liquid surface resides and therefore monitoring is constantly required while the probe is lowered toward the vessel.
- a reset signal is generated and a zero point of capacitance is set there.
- the capacitance gradually increases as the probe is inserted into and then lowered inside a deep sample vessel.
- a hump signal fluctuation is obtained.
- the analyzer captures the hump signal fluctuation, it recognizes the liquid surface.
- such a hump signal fluctuation also occurs owing to discharge noise or vibration generated while the probe is lowered and thereby incorrect surface detection will be made.
- the information on the place where the surface height is present can be obtained before the probe is lowered and therefore the reset signal is generated after the probe have approached the vicinity of the liquid surface (3 millimeters above the liquid surface). This makes it possible to ignore a hump signal occurring owing to discharge noise or vibration generated during lowering operation.
- the liquid surface can be correctly detected if discharge noise during lowering operation can be ignored.
- an electrolyte sample probe may be an electric probe, which can be easily inserted into the vessel. Therefore, it is the sample probe of an electrolyte analysis unit that is first inserted into the sample vessel. This sample probe correctly measures the surface height and transfers information on the height to another analysis unit for colorimetric measurement.
- Sharing between analysis units information about the sample and liquid surface in the sample vessel obtained in the inspection operation makes it possible to omit surface detection to be performed by subsequent analysis units, thus improving the analysis efficiency. Further, even when liquid surface detection (hereinafter referred to simply as surface detection) is not omitted, if surface height information obtained by an analysis unit differs from surface height information obtained by the subsequent analysis unit, it can be determined that incorrect surface detection has been made because of, for example, air bubbles produced on the liquid surface of the sample. Thus, more reliable analysis can be attained.
- FIG. 1 is a schematic diagram showing the overall configuration of an analysis unit according to the present invention.
- FIG. 2 is a schematic diagram showing the overall configuration of an automatic multi-purpose analyzer having a plurality of analysis units.
- FIG. 3 shows a problem to be solved by the present invention.
- FIG. 4 is a schematic diagram of the automatic multi-purpose analyzer according to the present invention.
- FIG. 5A is a graph showing a relation between the probe lowering speed and time
- FIG. 5B showing a relation between a surface detection signal output and time.
- FIG. 6 is a schematic diagram of an electric surface detection apparatus.
- An automatic multi-purpose analyzer pipettes sample liquid such as blood, urine, etc. and reagent liquid into a reaction vessel and analyzes the mixture thereof.
- a capacitive liquid level detection method has been used widely for liquid level detection because the outer diameter of its sample probe can be reduced. The reason the outer diameter reduction is necessary is that a reaction vessel has been remarkably reduced in size to about 2 mm ⁇ 4 mm because of reduced amounts of reaction liquid. Accordingly, a capacitive probe having an outer diameter of 1 millimeter or less is suitable for use as a sample probe that is inserted into such a small reaction vessel.
- a present modularized automatic multi-purpose analyzer commonly includes detection means for detecting a liquid surface level for each pipetting mechanism.
- detection means for detecting a liquid surface level for each pipetting mechanism In a sample pipetting mechanism of a modular analysis unit, even if a liquid surface level is misdetected due to discharge noises, that modular analysis unit alone cannot determine whether or not misdetection has occurred.
- a modular analysis unit shares with other modular analysis units liquid surface level information (amount of sample liquid) obtained by the analysis unit, which allows any of the analysis units to verify liquid surface level information obtained from the pipetting devises of other analysis units. This allows the automatic multi-purpose analyzer to avoid incorrect analysis caused by incorrect liquid surface level information.
- FIG. 1 is a schematic diagram of the periphery of pipetting mechanisms of a common automatic analyzer. Since the functions of respective sections are well-known, detailed description of the functions will be omitted.
- the automatic multi-purpose analyzer is configured such that a sample pipetting arm 2 of a sample pipetting mechanism 1 moves vertically and rotates, and a sample pipetting probe 105 attached to the sample pipetting arm 2 suctions a sample liquid 7 in a sample vessel 101 installed on a horizontally-rotating sample disk 102 and discharges the sample liquid 7 into a reaction vessel 106 . As shown in FIG.
- the sample disk 102 is typically universally designed to accommodate sample vessels; that is, a sample vessel 101 can be placed directly on the sample disk 102 , or the sample vessel 101 can be placed on a test tube (not shown) installed on the sample disk 102 .
- a rotatable reagent disk 125 installs thereon reagent bottles 112 , each being associated with a plurality of analysis items subjected to analysis.
- a reagent pipetting probe 110 attached to a movable arm pipettes a predetermined amount of reagent liquid from a reagent bottle 112 to a reaction vessel 106 .
- the sample pipetting probe 105 performs sample suction and discharge operations in response to the operation of a sample syringe pump 107 .
- the reagent pipetting probe 110 performs reagent suction and discharge operations in response to the operation of a reagent syringe pump 111 .
- Analysis items to be analyzed for each sample are input from input devices such as a keyboard 121 or the screen of a CRT 118 .
- the operation of each unit in the automatic multi-purpose analyzer is controlled by a computer 103 .
- a sample vessel 101 is transferred to a sample suction position, and the sample pipetting probe 105 is lowered into the sample vessel 101 in a halted state.
- a liquid surface level detector 151 outputs a detection signal, and the computer 103 performs control so as to stop the lowering operation by the drive unit of the movable sample pipetting arm 2 based on the detection signal. Then, the sample pipetting probe 105 suctions a predetermined amount of the sample liquid and rises to the upper dead center.
- a pressure detection circuit 153 monitors pressure fluctuation inside a passage between the sample pipetting probe 105 and the sample syringe pump 107 by use of a signal from a pressure sensor 152 . If an abnormal pressure fluctuation is detected during the suction operation, that means the predetermined amount of the sample liquid may not have been suctioned, and an alarm is therefore added to related analysis data.
- the sample pipetting arm 2 horizontally swings to lower the sample pipetting probe 105 at the position of a reaction vessel 106 on a reaction disk 109 , and the sample pipetting probe 105 discharges the sample liquid into the reaction vessel 106 .
- a reagent liquid associated with a relevant analysis item is added from the reagent pipetting probe 110 into the reaction vessel 106 .
- the liquid surface levels of the sample liquid in the sample vessel 101 and of the reagent liquid in the reagent bottle 112 are detected.
- the mixture of the sample and reagent in the reaction vessel is stirred by a stirring device 113 .
- the reaction vessel containing the mixture is then transferred to measurement means 162 .
- an actuator 160 opens shielding means, and the luminescence value or absorbance of the mixture is measured by a photo-multiplier 161 or photometer as the measurement means.
- the resultant luminescence signal passes through an A/D converter 116 and then is supplied to the computer 103 through an interface 104 to calculate concentrations for analysis items. Analysis results are printed out by a printer 117 through the interface 104 or displayed on the screen of the CRT 118 and, at the same time, stored in a hard disk 122 or memory.
- the reaction vessel 106 that completed the photometry is cleaned at the position of a cleaning mechanism 119 .
- a cleaning pump 120 supplies cleaning water to the reaction vessel while discharging waster water from the reaction vessel.
- three concentric rows of vessel holding sections are formed on the sample disk 102 so as to concentrically set sample vessels 101 in three rows, and a sample suction position for the sample pipetting probe 105 is provided in each concentric row.
- An example of an automatic multi-purpose analyzer configured with a plurality of analysis units connected in series will be explained below with reference to FIG. 2 .
- the plurality of analysis units having the above-mentioned functions are connected in series by a sample transfer unit.
- An analyzer control unit serves as a user interface of the automatic multi-purpose analyzer, and interfaces inside the automatic multi-purpose analyzer are connected via suitable communication means such as Ethernet (registered trademark).
- a sample vessel is loaded from the sample loading unit and then transferred by the sample transfer unit to an analysis unit which is requested for analysis.
- the sample vessel that completed analysis is suitably transferred to the sample unloading unit.
- FIG. 2 shows a specific example of two different sample transfer paths: one is for a case where only an analysis unit 1 ( 10 ) is requested for analysis, and the other for a case where the analysis unit 1 ( 10 ), an analysis unit 2 ( 11 ), and an analysis unit 4 ( 13 ) are requested for analysis.
- the sample transfer unit is requested to transfer a sample vessel 101 to the analysis unit 1 ( 10 ), the analysis unit 2 ( 11 ), and the analysis unit 4 ( 13 ) for analysis, as stated above for FIG. 2 .
- the sample vessel 101 requested by the analyzer control unit 16 , is loaded from the sample loading unit 14 and then supplied to the analysis unit 1 ( 10 ) for analysis.
- the sample pipetting probe 105 is lowered into the sample vessel 101 , the lowering operation by the drive unit of the movable arm (sampling arm) 2 is stopped, and the pipetting probe 105 suctions a predetermined amount of sample.
- the pipetting probe detects the liquid surface of the sample during the suction operation, the sample is transferred from the analysis unit 1 ( 10 ) to the analysis unit 2 ( 11 ) and then to the analysis unit 3 ( 12 ) so as to be subjected to pipetting operation by each individual analysis unit. Accordingly, even if the sample is normally detected by the analysis unit 1 ( 10 ), the sample is subjected to incorrect detection by the pipetting probe of the analysis unit 2 and then transferred to the sample unloading unit 15 , resulting in degraded reliability of overall automatic analysis.
- the analysis unit 1 ( 10 ) includes an electrolyte (Na+, K+, and Cl-ion) measurement apparatus. Since the sample probe 20 of the analysis unit 1 ( 10 ) is an electric probe 21 , the sample probe 20 is highly reliable and therefore almost never fail. Further, a detection signal obtained is clear because of the ON/OFF (conducting/nonconducting) detection method.
- a liquid surface level 22 can also be correctly recognized. Even if there is not request on electrolyte, the probe is inserted to measure the liquid surface level 22 and then lowered to a suction position 23 . The liquid surface level information is once transferred to the CPU of the apparatus control unit 16 controlling the entire automatic multi-purpose analyzer and then to the analysis unit 2 ( 11 ) therefrom.
- a pipetting probe 24 of the analysis unit 2 ( 11 ) is a capacitive probe having a small outer diameter, and therefore can be easily inserted into a reaction vessel.
- the liquid surface level information is transferred to the pipetting probe 24 of the analysis unit 2 ( 11 ). Based on the information, the pipetting probe 24 is lowered at high speed until it reaches a position 25 , 5 millimeters above a surface position 22 of the analysis unit 1 during sample suction operation. Then, the lowering speed of the pipetting probe 24 is slowed down until it reaches a position 26 , 2 millimeters the surface position 22 . The lowering operation is continued at a constant low speed and then a liquid surface 27 is detected. The pipetting probe 24 is stopped at a position 28 , 1.5 millimeters below the liquid surface.
- FIG. 5A is a graph showing a relation between the probe lowering speed and time
- FIG. 5A is a graph showing a relation between the probe lowering speed and time
- FIG. 5B showing a relation between a surface detection signal output and time.
- a conventional automatic multi-purpose analyzer immediately before lowering operation starts ( 45 ), a reset signal is generated when the tip of the probe is in the vicinity of the entrance of the sample vessel, and the output voltage at this timing is set as a zero point.
- a detection speed curve 41 of the conventional automatic multi-purpose analyzer indicates that the probe moves at a constant speed until it reaches the liquid surface while a speed curve 40 of the automatic multi-purpose analyzer according to the present invention indicates that the probe moves at high speed.
- a detection signal pulse curve of FIG. 5B the probe is lowered into the sample vessel while observing a detection signal.
- the detection signal When the detection signal reaches and exceeds a fixed value (threshold value 51 ), it is judged that the probe has come in contact with the liquid surface.
- a fixed value threshold value 51
- the capacitance of a charge-time pulse signal 49 gradually increases as the probe is lowered, and exceeds the threshold value 51 although the probe has not yet come in contact with the liquid surface. In this case, a portion B ( 44 ) is incorrectly detected.
- a hump waveform is generated in a pulse signal 48 at a portion A ( 43 ) during probe lowering operation. Also if the hump signal exceeds the threshold value 51 , incorrect surface detection results. Since a pulse signal 50 according to the present invention transmits the liquid surface level with a certain accuracy, a reset trigger signal of the surface detection signal is generated 2 millimeters above the liquid surface ( 42 ). With the charge-time pulse signal 49 , an arrow portion 46 is reacknowledged as a zero point; with the discharge-time pulse signal 48 , an arrow portion 47 is reacknowledged as a zero point.
- the probe 52 is vertically moved by a stepping motor. Therefore, it is necessary to lower the probe 52 while counting the number of pulses given to the motor and, when the number of pulses reaches a certain number, generate a reset trigger signal, and lowers the probe 52 into a sample vessel 53 .
- the signal increases only slightly by charge, and discharge does not take place, during a short time (and in a short distance) since the probe is 2 millimeters above the liquid surface until it comes in contact with the liquid surface, remarkably increasing the reliability of surface detection.
- the probe Using the zero point as a reference position of the pipetting start position of the analysis unit 2 ( 11 ), the probe detects the liquid surface 27 from the reference position, and surface information having correction for lowered liquid surface by sample suction 29 is transmitted to an analysis unit 4 ( 13 ).
- the analysis unit 4 ( 13 ) performs the same pipetting probe control as that performed by other analysis units. This makes it possible to reduce incorrect surface detection operations by the pipetting probe of each analysis unit to shorten the processing time, thus contributing to provision of an optimal operating environment for the automatic multi-purpose analyzer.
- the first analysis unit installs therein an electrolyte measurement unit, it is also possible to dispose a mechanism dedicated for surface detection for securely measuring the liquid surface level between the sample loading unit 14 and the first analysis unit, and transmit the surface information to each analysis unit.
- a configuration for surface detection as shown in FIG. 6 is also possible.
- an arm 30 is provided with two sample probes 31 in parallel with each other, and conduction between the two probes is monitored.
- reaction vessels 32 are placed at very small intervals, that is, about 3 millimeters; however, it is easy to insert the probes into a sample vessel 33 (having an inner diameter of 8 millimeters) with the original gap between nozzles.
- the liquid surface is preliminarily known. If the liquid surface is approximately known, the sample probe can be lowered at high speed and slowed down in the vicinity of the liquid surface and accordingly the pipetting time can be shortened, thus improving the analysis throughput of the automatic multi-purpose analyzer.
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Abstract
Description
- 1. Field of the Invention
- The present invention relates to an automatic multi-purpose analyzer which performs qualitative and quantitative analysis of biological samples such as blood, urine, etc. More particularly, the present invention relates to an automatic multi-purpose analyzer having a function for transferring a sample between a plurality of analysis units through a transfer apparatus.
- 2. Description of the Related Art
- With the excellent measurement reproducibility, quantitative characteristics, and rapid analysis capabilities, a remarkably increasing number of automatic analyzers are used mainly in inspection centers and large hospitals. In particular, inspection centers which collect samples from local minor hospitals and analyze the samples on behalf of these hospitals are demanding a high-throughput analyzer capable of analyzing a number of samples in a short time. In order to meet this demand, a modularized analyzer having a plurality of analysis units connected in series through a transfer line is commercially available. Such a modularized analyzer is described, for example, in Japanese Patent No. 2988362.
- An object of the present invention is to provide an automatic modularized multi-purpose analyzer that attains higher throughput.
- In order to attain the above-mentioned object, the present invention is configured as follows:
- An automatic multi-purpose analyzer having a plurality of analysis units connected in series through a transfer line for transferring sample liquid, each of the analysis units including a pipetting mechanism for pipetting sample liquid, wherein each of the analysis units includes a transmission mechanism for transmitting information about the amount of a sample liquid to other analysis units, the information being obtained upon sample pipetting by the pipetting mechanism of each of the analysis units
- An example will be explained below.
- A mechanism used for first detecting the liquid surface to recognize its height (hereinafter referred to as surface height or surface level interchangeably) securely measures the surface height. Such a mechanism is based on a reliable liquid surface method. Information on the surface height is transferred to another analysis unit in which a capacitive sample probe is inserted into and then lowered inside a vessel. With the capacitive probe, capacitance fluctuation from a certain timing is monitored and, when the liquid surface is judged, lowering operation of the probe is stopped. This timing is referred to as reset time. With a conventional analyzer, it is not possible to know the height of the vessel at which the liquid surface resides and therefore monitoring is constantly required while the probe is lowered toward the vessel.
- Therefore, when the tip of the sample probe almost reaches the entrance of the vessel, a reset signal is generated and a zero point of capacitance is set there. The capacitance gradually increases as the probe is inserted into and then lowered inside a deep sample vessel. When the probe comes in contact with the liquid surface, a hump signal fluctuation is obtained. When the analyzer captures the hump signal fluctuation, it recognizes the liquid surface. However, such a hump signal fluctuation also occurs owing to discharge noise or vibration generated while the probe is lowered and thereby incorrect surface detection will be made. With the present invention, the information on the place where the surface height is present can be obtained before the probe is lowered and therefore the reset signal is generated after the probe have approached the vicinity of the liquid surface (3 millimeters above the liquid surface). This makes it possible to ignore a hump signal occurring owing to discharge noise or vibration generated during lowering operation.
- The liquid surface can be correctly detected if discharge noise during lowering operation can be ignored.
- Fortunately, with a large-sized modularized automatic analyzer, a unit for measuring electrolyte in a sample is disposed, in many cases, on an upstream side of the transfer line for transferring the sample (because electrolyte measurement has urgency, that is, measurements should be obtained as soon as possible). Since a reaction vessel (dilution mixture vessel) into which the sample is discharged is a large-sized type, an electrolyte sample probe may be an electric probe, which can be easily inserted into the vessel. Therefore, it is the sample probe of an electrolyte analysis unit that is first inserted into the sample vessel. This sample probe correctly measures the surface height and transfers information on the height to another analysis unit for colorimetric measurement.
- Sharing between analysis units information about the sample and liquid surface in the sample vessel obtained in the inspection operation makes it possible to omit surface detection to be performed by subsequent analysis units, thus improving the analysis efficiency. Further, even when liquid surface detection (hereinafter referred to simply as surface detection) is not omitted, if surface height information obtained by an analysis unit differs from surface height information obtained by the subsequent analysis unit, it can be determined that incorrect surface detection has been made because of, for example, air bubbles produced on the liquid surface of the sample. Thus, more reliable analysis can be attained.
-
FIG. 1 is a schematic diagram showing the overall configuration of an analysis unit according to the present invention. -
FIG. 2 is a schematic diagram showing the overall configuration of an automatic multi-purpose analyzer having a plurality of analysis units. -
FIG. 3 shows a problem to be solved by the present invention. -
FIG. 4 is a schematic diagram of the automatic multi-purpose analyzer according to the present invention. -
FIG. 5A is a graph showing a relation between the probe lowering speed and time, andFIG. 5B showing a relation between a surface detection signal output and time. -
FIG. 6 is a schematic diagram of an electric surface detection apparatus. - An automatic multi-purpose analyzer pipettes sample liquid such as blood, urine, etc. and reagent liquid into a reaction vessel and analyzes the mixture thereof. In recent years, a capacitive liquid level detection method has been used widely for liquid level detection because the outer diameter of its sample probe can be reduced. The reason the outer diameter reduction is necessary is that a reaction vessel has been remarkably reduced in size to about 2 mm×4 mm because of reduced amounts of reaction liquid. Accordingly, a capacitive probe having an outer diameter of 1 millimeter or less is suitable for use as a sample probe that is inserted into such a small reaction vessel. Although an electric probe is most reliable because it is free from misdetection, this type of probe requires two electrodes, which increases the outer diameter to 4 millimeters; thus, the probe may not fit into a reaction vessel. Thus, the capacitive liquid level detection method has been used widely. With the capacitive liquid level detection method, discharge noises may occur depending on the charged state in the sample vessel, resulting in liquid level misdetection by a sample pipetting mechanism.
- A present modularized automatic multi-purpose analyzer commonly includes detection means for detecting a liquid surface level for each pipetting mechanism. In a sample pipetting mechanism of a modular analysis unit, even if a liquid surface level is misdetected due to discharge noises, that modular analysis unit alone cannot determine whether or not misdetection has occurred. In the automatic multi-purpose analyzer having multiple modular analysis units according to the present invention, a modular analysis unit shares with other modular analysis units liquid surface level information (amount of sample liquid) obtained by the analysis unit, which allows any of the analysis units to verify liquid surface level information obtained from the pipetting devises of other analysis units. This allows the automatic multi-purpose analyzer to avoid incorrect analysis caused by incorrect liquid surface level information.
- An embodiment of the present invention will be described below with reference to the accompanying drawings.
-
FIG. 1 is a schematic diagram of the periphery of pipetting mechanisms of a common automatic analyzer. Since the functions of respective sections are well-known, detailed description of the functions will be omitted. The automatic multi-purpose analyzer is configured such that asample pipetting arm 2 of asample pipetting mechanism 1 moves vertically and rotates, and asample pipetting probe 105 attached to thesample pipetting arm 2 suctions a sample liquid 7 in asample vessel 101 installed on a horizontally-rotatingsample disk 102 and discharges the sample liquid 7 into areaction vessel 106. As shown inFIG. 1 , thesample disk 102 is typically universally designed to accommodate sample vessels; that is, asample vessel 101 can be placed directly on thesample disk 102, or thesample vessel 101 can be placed on a test tube (not shown) installed on thesample disk 102. - The configuration of the automatic multi-purpose analyzer of
FIG. 1 will be explained below in more detail. Arotatable reagent disk 125 installs thereonreagent bottles 112, each being associated with a plurality of analysis items subjected to analysis. Areagent pipetting probe 110 attached to a movable arm pipettes a predetermined amount of reagent liquid from areagent bottle 112 to areaction vessel 106. - The
sample pipetting probe 105 performs sample suction and discharge operations in response to the operation of asample syringe pump 107. Thereagent pipetting probe 110 performs reagent suction and discharge operations in response to the operation of areagent syringe pump 111. Analysis items to be analyzed for each sample are input from input devices such as akeyboard 121 or the screen of aCRT 118. The operation of each unit in the automatic multi-purpose analyzer is controlled by acomputer 103. - With the intermittent rotation of the
sample disk 102, asample vessel 101 is transferred to a sample suction position, and thesample pipetting probe 105 is lowered into thesample vessel 101 in a halted state. When the tip of thesample pipetting probe 105 comes in contact with the surface of the sample liquid with the lowering operation of thesample pipetting probe 105, a liquidsurface level detector 151 outputs a detection signal, and thecomputer 103 performs control so as to stop the lowering operation by the drive unit of the movablesample pipetting arm 2 based on the detection signal. Then, thesample pipetting probe 105 suctions a predetermined amount of the sample liquid and rises to the upper dead center. While thesample pipetting probe 105 is suctioning a predetermined amount of the sample liquid, apressure detection circuit 153 monitors pressure fluctuation inside a passage between thesample pipetting probe 105 and thesample syringe pump 107 by use of a signal from apressure sensor 152. If an abnormal pressure fluctuation is detected during the suction operation, that means the predetermined amount of the sample liquid may not have been suctioned, and an alarm is therefore added to related analysis data. - Then, the
sample pipetting arm 2 horizontally swings to lower thesample pipetting probe 105 at the position of areaction vessel 106 on areaction disk 109, and thesample pipetting probe 105 discharges the sample liquid into thereaction vessel 106. When thereaction vessel 106 containing the sample is moved to a reagent addition position, a reagent liquid associated with a relevant analysis item is added from thereagent pipetting probe 110 into thereaction vessel 106. During the sample and reagent pipetting operations, the liquid surface levels of the sample liquid in thesample vessel 101 and of the reagent liquid in thereagent bottle 112 are detected. The mixture of the sample and reagent in the reaction vessel is stirred by a stirringdevice 113. The reaction vessel containing the mixture is then transferred to measurement means 162. At the same time, an actuator 160 opens shielding means, and the luminescence value or absorbance of the mixture is measured by a photo-multiplier 161 or photometer as the measurement means. The resultant luminescence signal passes through an A/D converter 116 and then is supplied to thecomputer 103 through aninterface 104 to calculate concentrations for analysis items. Analysis results are printed out by aprinter 117 through theinterface 104 or displayed on the screen of theCRT 118 and, at the same time, stored in ahard disk 122 or memory. Thereaction vessel 106 that completed the photometry is cleaned at the position of acleaning mechanism 119. Acleaning pump 120 supplies cleaning water to the reaction vessel while discharging waster water from the reaction vessel. In the example ofFIG. 1 , three concentric rows of vessel holding sections are formed on thesample disk 102 so as to concentrically setsample vessels 101 in three rows, and a sample suction position for thesample pipetting probe 105 is provided in each concentric row. - An example of an automatic multi-purpose analyzer configured with a plurality of analysis units connected in series will be explained below with reference to
FIG. 2 . The plurality of analysis units having the above-mentioned functions are connected in series by a sample transfer unit. An analyzer control unit serves as a user interface of the automatic multi-purpose analyzer, and interfaces inside the automatic multi-purpose analyzer are connected via suitable communication means such as Ethernet (registered trademark). A sample vessel is loaded from the sample loading unit and then transferred by the sample transfer unit to an analysis unit which is requested for analysis. The sample vessel that completed analysis is suitably transferred to the sample unloading unit.FIG. 2 shows a specific example of two different sample transfer paths: one is for a case where only an analysis unit 1 (10) is requested for analysis, and the other for a case where the analysis unit 1 (10), an analysis unit 2 (11), and an analysis unit 4 (13) are requested for analysis. - Problems with present automatic multi-purpose analyzers will be explained below with reference to
FIG. 3 . Assume that the sample transfer unit is requested to transfer asample vessel 101 to the analysis unit 1 (10), the analysis unit 2 (11), and the analysis unit 4 (13) for analysis, as stated above forFIG. 2 . Thesample vessel 101, requested by theanalyzer control unit 16, is loaded from thesample loading unit 14 and then supplied to the analysis unit 1 (10) for analysis. As mentioned above, thesample pipetting probe 105 is lowered into thesample vessel 101, the lowering operation by the drive unit of the movable arm (sampling arm) 2 is stopped, and thepipetting probe 105 suctions a predetermined amount of sample. If the pipetting probe detects the liquid surface of the sample during the suction operation, the sample is transferred from the analysis unit 1 (10) to the analysis unit 2 (11) and then to the analysis unit 3 (12) so as to be subjected to pipetting operation by each individual analysis unit. Accordingly, even if the sample is normally detected by the analysis unit 1 (10), the sample is subjected to incorrect detection by the pipetting probe of theanalysis unit 2 and then transferred to thesample unloading unit 15, resulting in degraded reliability of overall automatic analysis. - The operation of the automatic multi-purpose analyzer according to the present invention will be explained below with reference to
FIGS. 3 and 4 . - The analysis unit 1 (10) includes an electrolyte (Na+, K+, and Cl-ion) measurement apparatus. Since the
sample probe 20 of the analysis unit 1 (10) is anelectric probe 21, thesample probe 20 is highly reliable and therefore almost never fail. Further, a detection signal obtained is clear because of the ON/OFF (conducting/nonconducting) detection method. - A
liquid surface level 22 can also be correctly recognized. Even if there is not request on electrolyte, the probe is inserted to measure theliquid surface level 22 and then lowered to asuction position 23. The liquid surface level information is once transferred to the CPU of theapparatus control unit 16 controlling the entire automatic multi-purpose analyzer and then to the analysis unit 2 (11) therefrom. Apipetting probe 24 of the analysis unit 2 (11) is a capacitive probe having a small outer diameter, and therefore can be easily inserted into a reaction vessel. - The liquid surface level information is transferred to the
pipetting probe 24 of the analysis unit 2 (11). Based on the information, thepipetting probe 24 is lowered at high speed until it reaches a 25, 5 millimeters above aposition surface position 22 of theanalysis unit 1 during sample suction operation. Then, the lowering speed of thepipetting probe 24 is slowed down until it reaches a 26, 2 millimeters theposition surface position 22. The lowering operation is continued at a constant low speed and then aliquid surface 27 is detected. Thepipetting probe 24 is stopped at aposition 28, 1.5 millimeters below the liquid surface.FIG. 5A is a graph showing a relation between the probe lowering speed and time, andFIG. 5B showing a relation between a surface detection signal output and time. With a conventional automatic multi-purpose analyzer, immediately before lowering operation starts (45), a reset signal is generated when the tip of the probe is in the vicinity of the entrance of the sample vessel, and the output voltage at this timing is set as a zero point. InFIG. 5A , adetection speed curve 41 of the conventional automatic multi-purpose analyzer indicates that the probe moves at a constant speed until it reaches the liquid surface while aspeed curve 40 of the automatic multi-purpose analyzer according to the present invention indicates that the probe moves at high speed. With a detection signal pulse curve ofFIG. 5B , the probe is lowered into the sample vessel while observing a detection signal. When the detection signal reaches and exceeds a fixed value (threshold value 51), it is judged that the probe has come in contact with the liquid surface. However, depending on the charging state in the sample vessel (in particular, a plastic blood collection pipe is easy to be charged and, after a centrifuge or the like is used for serum separation, the blood collection pipe is charged very intensively), the capacitance of a charge-time pulse signal 49 gradually increases as the probe is lowered, and exceeds thethreshold value 51 although the probe has not yet come in contact with the liquid surface. In this case, a portion B (44) is incorrectly detected. If discharge takes place between the sample vessel inner surface and the probe, a hump waveform is generated in apulse signal 48 at a portion A (43) during probe lowering operation. Also if the hump signal exceeds thethreshold value 51, incorrect surface detection results. Since apulse signal 50 according to the present invention transmits the liquid surface level with a certain accuracy, a reset trigger signal of the surface detection signal is generated 2 millimeters above the liquid surface (42). With the charge-time pulse signal 49, anarrow portion 46 is reacknowledged as a zero point; with the discharge-time pulse signal 48, anarrow portion 47 is reacknowledged as a zero point. - The
probe 52 is vertically moved by a stepping motor. Therefore, it is necessary to lower theprobe 52 while counting the number of pulses given to the motor and, when the number of pulses reaches a certain number, generate a reset trigger signal, and lowers theprobe 52 into asample vessel 53. - Since capacitance fluctuations from the reacknowledged zero points are monitored, the signal increases only slightly by charge, and discharge does not take place, during a short time (and in a short distance) since the probe is 2 millimeters above the liquid surface until it comes in contact with the liquid surface, remarkably increasing the reliability of surface detection.
- Using the zero point as a reference position of the pipetting start position of the analysis unit 2 (11), the probe detects the
liquid surface 27 from the reference position, and surface information having correction for lowered liquid surface bysample suction 29 is transmitted to an analysis unit 4 (13). The analysis unit 4 (13) performs the same pipetting probe control as that performed by other analysis units. This makes it possible to reduce incorrect surface detection operations by the pipetting probe of each analysis unit to shorten the processing time, thus contributing to provision of an optimal operating environment for the automatic multi-purpose analyzer. - Although the first analysis unit installs therein an electrolyte measurement unit, it is also possible to dispose a mechanism dedicated for surface detection for securely measuring the liquid surface level between the
sample loading unit 14 and the first analysis unit, and transmit the surface information to each analysis unit. - A configuration for surface detection as shown in
FIG. 6 is also possible. In the first analysis unit, anarm 30 is provided with twosample probes 31 in parallel with each other, and conduction between the two probes is monitored. Recently,reaction vessels 32 are placed at very small intervals, that is, about 3 millimeters; however, it is easy to insert the probes into a sample vessel 33 (having an inner diameter of 8 millimeters) with the original gap between nozzles. - As means for first inserting the probe into the vessel to measure the liquid surface, it is also possible to lower the probe while discharging air from the tip of the nozzle and detect pressure fluctuation inside the nozzle at the moment when the probe comes in contact with the liquid surface.
- There is another advantage if the liquid surface is preliminarily known. If the liquid surface is approximately known, the sample probe can be lowered at high speed and slowed down in the vicinity of the liquid surface and accordingly the pipetting time can be shortened, thus improving the analysis throughput of the automatic multi-purpose analyzer.
Claims (8)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2007224998A JP4538478B2 (en) | 2007-08-31 | 2007-08-31 | Automatic analyzer |
| JP2007-224998 | 2007-08-31 |
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| US20090060785A1 true US20090060785A1 (en) | 2009-03-05 |
| US8075840B2 US8075840B2 (en) | 2011-12-13 |
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| US12/200,459 Active 2029-04-25 US8075840B2 (en) | 2007-08-31 | 2008-08-28 | Automatic multi-purpose analyzer |
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| Country | Link |
|---|---|
| US (1) | US8075840B2 (en) |
| EP (1) | EP2031409B1 (en) |
| JP (1) | JP4538478B2 (en) |
| CN (1) | CN101377520B (en) |
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| US20120039771A1 (en) * | 2009-01-30 | 2012-02-16 | Hitachi High-Technologies Corporation | Automatic analyzer and sample treatment apparatus |
| US9470570B2 (en) | 2011-09-20 | 2016-10-18 | Hitachi High-Technologies Corporation | Automatic analyzer and method for determining malfunction thereof |
| US20160313362A1 (en) * | 2013-12-16 | 2016-10-27 | Shimadzu Corporation | Liquid collection device and automated analyzer provided therewith |
| US10288637B2 (en) * | 2014-05-15 | 2019-05-14 | Hitachi High-Technologies Corporation | Automatic analyzer |
| US11125678B2 (en) | 2006-06-02 | 2021-09-21 | Luminex Corporation | Systems and methods for performing measurements of one or more materials |
| US20220196696A1 (en) * | 2020-12-21 | 2022-06-23 | Tecan Trading Ag | Iterative liquid aspiration |
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| JP2010286325A (en) * | 2009-06-10 | 2010-12-24 | Beckman Coulter Inc | Dispensing device, automatic analyzer and liquid level detection method |
| JP5308952B2 (en) * | 2009-07-27 | 2013-10-09 | 株式会社日立ハイテクノロジーズ | Automatic analyzer |
| JP5570848B2 (en) * | 2010-03-05 | 2014-08-13 | 株式会社東芝 | Automatic analyzer |
| GB2501056B (en) | 2012-02-06 | 2016-11-02 | Stratec Biomedical Ag | Liquid level monitoring |
| JP5993652B2 (en) * | 2012-08-03 | 2016-09-14 | 株式会社日立ハイテクノロジーズ | Automatic analyzer |
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| US11125678B2 (en) | 2006-06-02 | 2021-09-21 | Luminex Corporation | Systems and methods for performing measurements of one or more materials |
| US20120039771A1 (en) * | 2009-01-30 | 2012-02-16 | Hitachi High-Technologies Corporation | Automatic analyzer and sample treatment apparatus |
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| US20160313362A1 (en) * | 2013-12-16 | 2016-10-27 | Shimadzu Corporation | Liquid collection device and automated analyzer provided therewith |
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Also Published As
| Publication number | Publication date |
|---|---|
| JP2009058323A (en) | 2009-03-19 |
| EP2031409A3 (en) | 2010-09-22 |
| EP2031409A2 (en) | 2009-03-04 |
| JP4538478B2 (en) | 2010-09-08 |
| CN101377520B (en) | 2013-06-12 |
| CN101377520A (en) | 2009-03-04 |
| EP2031409B1 (en) | 2012-10-31 |
| US8075840B2 (en) | 2011-12-13 |
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